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多异质结复合光催化剂的高效稳定光催化析氢活性:CdS和NiS共修饰的NaNbO纳米立方体

Efficient and Stable Photocatalytic Hydrogen Evolution Activity of Multi-Heterojunction Composite Photocatalysts: CdS and NiS Co-modified NaNbO Nanocubes.

作者信息

Xu Jingjing, Zhu Jiawei, Niu Junfeng, Chen Mindong, Yue Junpeng

机构信息

Jiangsu Key Laboratory of Atmospheric Environment Monitoring and Pollution Control, Collaborative Innovation Center of Atmospheric Environment and Equipment Technology, Jiangsu Engineering Technology Research Center of Environmental Cleaning Materials, School of Environmental Science and Engineering, Nanjing University of Information Science and Technology, Nanjing, China.

Research Center for Eco-Environmental Engineering, Dongguan University of Technology, Dongguan, China.

出版信息

Front Chem. 2020 Jan 21;7:880. doi: 10.3389/fchem.2019.00880. eCollection 2019.

Abstract

In this study, a NaNbO/CdS/NiS ternary composite photocatalyst containing no precious metals was successfully prepared by a simple hydrothermal method. The prepared ternary photocatalyst has a significant improvement in photocatalytic performance of hydrogen production from water splitting under visible light irradiation. The best sample NCN40% hydrogen production rate is 4.698 mmol g h, which is about 24.7 times that of pure CdS sample. In addition, the stability of the composite catalyst in the long-term photocatalytic hydrogen production cycle is also improved. The reason for the enhanced hydrogen production performance may be the optimization of the microstructure of the catalyst and the reduction of photogenerated electron-hole recombination. The construction of multi-heterojunctions (NaNbO-CdS, CdS-NiS, and NaNbO-NiS) helps to reduce the recombination of carriers. Furthermore, the -formed NiS nanoparticles can serve as active sites for hydrogen evolution. All of these factors induced the improved photocatalytic activity of the as-prepared ternary photocatalyst.

摘要

在本研究中,通过简单的水热法成功制备了一种不含贵金属的NaNbO/CdS/NiS三元复合光催化剂。所制备的三元光催化剂在可见光照射下光催化水分解产氢性能有显著提高。最佳样品NCN40%的产氢速率为4.698 mmol g h,约为纯CdS样品的24.7倍。此外,复合催化剂在长期光催化产氢循环中的稳定性也得到了提高。产氢性能增强的原因可能是催化剂微观结构的优化以及光生电子-空穴复合的减少。多异质结(NaNbO-CdS、CdS-NiS和NaNbO-NiS)的构建有助于减少载流子的复合。此外,形成的NiS纳米颗粒可作为析氢的活性位点。所有这些因素导致了所制备的三元光催化剂光催化活性的提高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8724/6985095/40d7f61a31c4/fchem-07-00880-g0001.jpg

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